Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_assertion description "[To better define the deleted chromosomal loci and understand the genetic instability in EC tissues, we selected 12 microsatellite markers (D3S1232, D3S1238, D3S1289, D3S1480, D3S647, D3S966, D3S1317, D3S659, D9S156, D9S171, D9S176 and GSN) to examine 36 paired EC tissues for loss of heterozygosity (LOH) and microsatellite instability (MIN) on chromosomes 3 and 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_assertion evidence source_evidence_literature NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_assertion SIO_000772 8637728 NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_assertion wasDerivedFrom befree-2016 NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_assertion wasGeneratedBy ECO_0000203 NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1350211.RAm093FKUlOGIhL1DMipk73f3LaiPLCvgGUdVPSRCWxKo130_provenance.